Stereocenter: Difference between revisions
section on configuration |
MadeOfAtoms (talk | contribs) Restored revision 1196214220 by Philipnelson99 (talk): Test or vandalism |
||
| (28 intermediate revisions by 12 users not shown) | |||
| Line 6: | Line 6: | ||
[[File:Chirality with hands.svg|upright=1.3|thumb|Two [[enantiomer]]s of a generic [[amino acid]] at the stereocenter]] |
[[File:Chirality with hands.svg|upright=1.3|thumb|Two [[enantiomer]]s of a generic [[amino acid]] at the stereocenter]] |
||
In [[stereochemistry]], a '''stereocenter |
In [[stereochemistry]], a '''stereocenter''' of a [[molecule]] is an [[atom]] (center), axis or plane that is the focus of [[stereoisomerism]]; that is, when having at least three different groups bound to the stereocenter, interchanging any two different groups creates a new [[stereoisomer]].<ref name=":1">{{Cite web | url = https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Smith)/Chapter_05%3A_Stereochemistry/5.04_Stereogenic_Centers | title = 5.4: Stereogenic Centers | website = libretexts.org| date = April 24, 2015 }}</ref><ref name="Mislow&Siegel 1984">{{Cite journal |last1=Mislow |first1=Kurt |last2=Siegel |first2=Jay |year=1984 |title=Stereoisomerism and local chirality |journal=Journal of the American Chemical Society |volume=106 |issue=11 |pages=3319 |doi=10.1021/ja00323a043}}</ref> Stereocenters are also referred to as '''stereogenic centers'''. |
||
A |
A stereocenter is geometrically defined as a point (location) in a molecule; a stereocenter is usually but not always a specific atom, often carbon.<ref name="Mislow&Siegel 1984" /><ref name="solomons">{{Cite book | first1= T. W. Graham |last1= Solomons| first2= Craig | last2= Fryhle| publisher= John Wiley & Sons| year= 2004 | title = Organic Chemistry | edition = 8th }}{{page needed| date= February 2016}}</ref> Stereocenters can exist on [[Chirality (chemistry)|chiral]] or [[achiral]] molecules; stereocenters can contain single bonds or double bonds.<ref name=":1" /> The number of hypothetical stereoisomers can be predicted by using 2<sup>''n''</sup>, with ''n'' being the number of [[Tetrahedral molecular geometry|tetrahedral]] stereocenters; however, exceptions such as [[Meso compound|meso compounds]] can reduce the prediction to below the expected 2<sup>''n''</sup>.<ref name=":3" /> |
||
[[Chirality (chemistry)|'''Chirality centers''']] are a type of stereocenter with four different substituent groups; chirality centers are a specific subset of stereocenters because they can only have sp<sup>3</sup> hybridization, meaning that they can only have [[Sigma bond|single bonds]].<ref name=":2" /> |
|||
== Location == |
== Location == |
||
Stereocenters can exist on chiral or achiral molecules. A stereocenter can have either four different attachment groups, or three different attachment groups where one group is connected by a double bond.<ref name=":1" /> Since stereocenters can exist on achiral molecules, stereocenters can have either sp<sup>3</sup> or sp<sup>2</sup> hybridization. |
Stereocenters can exist on [[Chirality|chiral]] or [[achiral]] molecules. They are defined as a location (point) within a molecule, rather than a particular atom, in which the interchanging of two groups creates a stereoisomer.<ref name="solomons" /> A stereocenter can have either four different attachment groups, or three different attachment groups where one group is connected by a double bond.<ref name=":1" /> Since stereocenters can exist on achiral molecules, stereocenters can have either [[Hybridization (chemistry)|sp<sup>3</sup> or sp<sup>2</sup> hybridization]]. |
||
==Possible Number of Stereoisomers== |
==Possible Number of Stereoisomers== |
||
Stereoisomers are compounds that are identical in composition and connectivity but have a different spatial arrangement of atoms around the central atom.<ref name=":0">{{Cite book | |
Stereoisomers are compounds that are identical in composition and connectivity but have a different spatial arrangement of atoms around the central atom.<ref name=":0">{{Cite book |last1=Brown |first1=William |title=Organic Chemistry |last2=Iverson |first2=Brent |last3=Anslyn |first3=Eric |last4=Foote |first4=Christopher |publisher=Cengage Learning |year=2018 |isbn=978-1-305-58035-0 |edition=8th |location=Boston, MA |pages=117,137–139}}</ref> A molecule having multiple stereocenters will produce many possible stereoisomers. In compounds whose stereoisomerism is due to [[Tetrahedral molecular geometry|tetrahedral]] (sp<sup>3</sup>) stereogenic centers, the total number of hypothetically possible stereoisomers will not exceed 2<sup>''n''</sup>, where ''n'' is the number of tetrahedral stereocenters. However, this is an upper bound because molecules with symmetry frequently have fewer stereoisomers. |
||
The stereoisomers produced by the presence of multiple stereocenters can be defined as [[Enantiomer|enantiomers]] (non- |
The stereoisomers produced by the presence of multiple stereocenters can be defined as [[Enantiomer|enantiomers]] (non-superposable mirror images) and [[Diastereomer|diastereomers]] (non-superposable, non-identical, non-mirror image molecules).<ref name=":0" /> Enantiomers and diastereomers are produced due to differing [[Cahn–Ingold–Prelog priority rules|stereochemical configurations]] of molecules containing the same composition and connectivity (bonding); the molecules must have multiple (two or more) stereocenters to be classified as enantiomers or diastereomers. Enantiomers and diastereomers will produce individual stereoisomers that contribute to the total number of possible stereoisomers. |
||
However, the stereoisomers produced may also give a [[meso compound]], which is an achiral compound that is |
However, the stereoisomers produced may also give a [[meso compound]], which is an achiral compound that is [[Chirality (chemistry)|superposable]] on its mirror image; the presence of a meso compound will reduce the number of possible stereoisomers.<ref name=":3">{{Cite journal |last=Soderberg |first=Timothy |date=2019-07-01 |title=Organic Chemistry with a Biological Emphasis Volume I |url=https://digitalcommons.morris.umn.edu/chem_facpubs/1 |journal=Chemistry Publications |pages=170,177}}</ref> Since a meso compound is superposable on its mirror image, the two "stereoisomers" are actually identical. Resultantly, a meso compound will reduce the number of stereoisomers to below the hypothetical 2<sup>''n''</sup> amount due to symmetry.<ref name=":0" /> |
||
Additionally, certain configurations may not exist due to steric reasons. Cyclic compounds with chiral centers may not exhibit chirality due to the presence of a two-fold rotation axis. [[Planar chirality]] may also provide for chirality without having an actual chiral center present. |
Additionally, certain configurations may not exist due to [[Steric effects|steric]] reasons. [[Cyclic compound|Cyclic compounds]] with chiral centers may not exhibit chirality due to the presence of a two-fold rotation axis. [[Planar chirality]] may also provide for chirality without having an actual chiral center present. |
||
== Configuration == |
== Configuration == |
||
Configuration is defined as the arrangement of atoms around a stereocenter.<ref name=":0" /> The [[Cahn–Ingold–Prelog priority rules|Cahn-Ingold-Prelog]] (CIP) system uses R and S designations to define the configuration of atoms about any stereocenter.<ref name=":12">{{Cite journal | |
Configuration is defined as the arrangement of atoms around a stereocenter.<ref name=":0" /> The [[Cahn–Ingold–Prelog priority rules|Cahn-Ingold-Prelog]] (CIP) system uses R and S designations to define the configuration of atoms about any stereocenter.<ref name=":12">{{Cite journal |last1=Barta |first1=Nancy S. |last2=Stille |first2=John R. |date=1994 |title=Grasping the Concepts of Stereochemistry |url=https://pubs.acs.org/doi/abs/10.1021/ed071p20 |journal=Journal of Chemical Education |language= |volume=71 |issue=1 |page=20 |doi=10.1021/ed071p20 |bibcode=1994JChEd..71...20B |issn=0021-9584|url-access=subscription }}</ref> A designation of R denotes a clockwise direction of substituent priority around the stereocenter, while a designation of S denotes a counter-clockwise direction of substituent priority.<ref name=":12" /> |
||
==Chirality Centers== |
==Chirality Centers== |
||
A |
A [[Chirality (chemistry)|chirality center]] (chiral center) is a type of stereocenter. A chirality center is defined as an atom holding a set of four different [[ligand|ligands]] (atoms or groups of atoms) in a spatial arrangement which is non-superposable on its mirror image. Chirality centers must be sp<sup>3</sup> hybridized, meaning that a chirality center can only have [[Sigma bond|single bonds]].<ref name=":2">{{Cite web |date=2021-12-15 |title=5.3: Chirality and R/S Naming System |url=https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Liu)/05%3A_Stereochemistry/5.03%3A_Chirality_and_R_S_Naming_System |access-date=2022-11-12 |website=Chemistry LibreTexts |language=en}}</ref> In [[organic chemistry]], a chirality center usually refers to a [[carbon]], [[phosphorus]], or [[sulfur]] atom, though it is also possible for other atoms to be chirality centers, especially in areas of [[organometallic]] and [[inorganic chemistry]]. |
||
The concept of a chirality center generalizes the concept of an [[asymmetric carbon|asymmetric carbon atom]] (a carbon atom bonded to four different entities) to a broader definition of any atom with four different attachment groups in which an interchanging of any two attachment groups gives rise to an [[enantiomer]].<ref>{{Cite journal |title=chiral (chirality) center |url=http://goldbook.iupac.org/C01060.html |website=[[IUPAC]].org|doi=10.1351/goldbook.C01060 |doi-access=free }}</ref> |
|||
==Stereogenic on |
==Stereogenic on Carbon== |
||
A carbon atom that is attached to four different substituent groups is called an ''[[Asymmetric carbon|asymmetric carbon atom]]'' or ''chiral carbon''. |
A carbon atom that is attached to four different substituent groups is called an ''[[Asymmetric carbon|asymmetric carbon atom]]'' or ''chiral carbon''. Chiral carbons are the most common type of chirality center.<ref name=":0" /> |
||
==Stereogenic on |
==Stereogenic on Other Atoms== |
||
Chirality is not limited to carbon atoms, though carbon atoms are often centers of chirality due to their ubiquity in organic chemistry. Nitrogen and phosphorus atoms can also form bonds in a tetrahedral configuration. A nitrogen in an [[amine]] may be a stereocenter if all three groups attached are different because the [[electron pair]] of the amine functions as a fourth group.<ref name=OChemSmith>{{cite book |last1=Smith |first1=Janice Gorzynski |editor1-last=Hodge |editor1-first=Tami |editor2-last=Nemmers |editor2-first=Donna |editor3-last=Klein |editor3-first=Jayne |title=Organic chemistry |date=2011 |publisher=McGraw-Hill |location=New York, NY |isbn=978-0-07-337562-5 |pages=949–993 |edition=3rd |url=http://highered.mheducation.com/sites/007340277x/student_view0/index.html |language=en |format=Book |chapter=Chapter 25 Amines}}</ref> However, [[nitrogen inversion]], a form of [[pyramidal inversion]], causes [[racemization]] which means that both [[epimers]] at that nitrogen are present under normal circumstances.<ref name="OChemSmith" /> Racemization by [[nitrogen inversion]] may be restricted (such as [[quaternary ammonium cation|quaternary ammonium]] or [[phosphonium]] cations), or slow, which allows the existence of chirality.<ref name="OChemSmith" /> |
Chirality is not limited to carbon atoms, though carbon atoms are often centers of chirality due to their ubiquity in organic chemistry. Nitrogen and phosphorus atoms can also form bonds in a tetrahedral configuration. A nitrogen in an [[amine]] may be a stereocenter if all three groups attached are different because the [[electron pair]] of the amine functions as a fourth group.<ref name=OChemSmith>{{cite book |last1=Smith |first1=Janice Gorzynski |editor1-last=Hodge |editor1-first=Tami |editor2-last=Nemmers |editor2-first=Donna |editor3-last=Klein |editor3-first=Jayne |title=Organic chemistry |date=2011 |publisher=McGraw-Hill |location=New York, NY |isbn=978-0-07-337562-5 |pages=949–993 |edition=3rd |url=http://highered.mheducation.com/sites/007340277x/student_view0/index.html |language=en |format=Book |chapter=Chapter 25 Amines}}</ref> However, [[nitrogen inversion]], a form of [[pyramidal inversion]], causes [[racemization]] which means that both [[epimers]] at that nitrogen are present under normal circumstances.<ref name="OChemSmith" /> Racemization by [[nitrogen inversion]] may be restricted (such as [[quaternary ammonium cation|quaternary ammonium]] or [[phosphonium]] cations), or slow, which allows the existence of chirality.<ref name="OChemSmith" /> |
||
Metal atoms with tetrahedral or [[octahedral molecular geometry|octahedral]] geometries may also be chiral due to having different ligands. For the octahedral case, several chiralities are possible. Having three ligands of two types, the ligands may be lined up along the meridian, giving the ''mer''-isomer, or forming a face—the ''fac'' isomer. Having three bidentate ligands of only one type gives a propeller-type structure, with two different enantiomers denoted Λ and Δ. |
Metal atoms with tetrahedral or [[octahedral molecular geometry|octahedral]] geometries may also be chiral due to having different ligands. For the octahedral case, several chiralities are possible. Having three ligands of two types, the ligands may be lined up along the meridian, giving the ''mer''-isomer, or forming a face—the ''fac'' isomer. Having three bidentate ligands of only one type gives a propeller-type structure, with two different enantiomers denoted Λ and Δ. |
||
== Chirality and Stereocenters == |
|||
As mentioned earlier, the requirement for an atom to be a chirality center is that the atom must be sp<sup>3</sup> hybridized with four different attachments.<ref name=":2" /> Because of this, all chirality centers are stereocenters. However, only under some conditions is the reverse true. Recall that a point can be considered a sterocenter with a minimum of three attachment points; stereocenters can be either sp<sup>3</sup> or sp<sup>2</sup> hybridized, as long as the interchanging any two different groups creates a new [[stereoisomer]]. This means that although all chirality centers are stereocenters, not every stereocenter is a chirality center. |
|||
Stereocenters are important identifiers for chiral or achiral molecules. As a general rule, if a molecule has no stereocenters, it is considered achiral. If it has at least one stereocenter, the molecule has the potential for chirality. However, there are some exceptions like [[Meso compound|meso compounds]] that make molecules with multiple stereocenters considered achiral.<ref name=":0" /> |
|||
==See also== |
==See also== |
||
Latest revision as of 09:48, 3 April 2024
 | This article has multiple issues. Please help improve it or discuss these issues on the talk page. (Learn how and when to remove these template messages)
|
In stereochemistry, a stereocenter of a molecule is an atom (center), axis or plane that is the focus of stereoisomerism; that is, when having at least three different groups bound to the stereocenter, interchanging any two different groups creates a new stereoisomer.[1][2] Stereocenters are also referred to as stereogenic centers.
A stereocenter is geometrically defined as a point (location) in a molecule; a stereocenter is usually but not always a specific atom, often carbon.[2][3] Stereocenters can exist on chiral or achiral molecules; stereocenters can contain single bonds or double bonds.[1] The number of hypothetical stereoisomers can be predicted by using 2n, with n being the number of tetrahedral stereocenters; however, exceptions such as meso compounds can reduce the prediction to below the expected 2n.[4]
Chirality centers are a type of stereocenter with four different substituent groups; chirality centers are a specific subset of stereocenters because they can only have sp3 hybridization, meaning that they can only have single bonds.[5]
Standort
[edit]Stereocenters can exist on chiral or achiral molecules. They are defined as a location (point) within a molecule, rather than a particular atom, in which the interchanging of two groups creates a stereoisomer.[3] A stereocenter can have either four different attachment groups, or three different attachment groups where one group is connected by a double bond.[1] Since stereocenters can exist on achiral molecules, stereocenters can have either sp3 or sp2 hybridization.
Possible Number of Stereoisomers
[edit]Stereoisomers are compounds that are identical in composition and connectivity but have a different spatial arrangement of atoms around the central atom.[6] A molecule having multiple stereocenters will produce many possible stereoisomers. In compounds whose stereoisomerism is due to tetrahedral (sp3) stereogenic centers, the total number of hypothetically possible stereoisomers will not exceed 2n, where n is the number of tetrahedral stereocenters. However, this is an upper bound because molecules with symmetry frequently have fewer stereoisomers.
The stereoisomers produced by the presence of multiple stereocenters can be defined as enantiomers (non-superposable mirror images) and diastereomers (non-superposable, non-identical, non-mirror image molecules).[6] Enantiomers and diastereomers are produced due to differing stereochemical configurations of molecules containing the same composition and connectivity (bonding); the molecules must have multiple (two or more) stereocenters to be classified as enantiomers or diastereomers. Enantiomers and diastereomers will produce individual stereoisomers that contribute to the total number of possible stereoisomers.
However, the stereoisomers produced may also give a meso compound, which is an achiral compound that is superposable on its mirror image; the presence of a meso compound will reduce the number of possible stereoisomers.[4] Since a meso compound is superposable on its mirror image, the two "stereoisomers" are actually identical. Resultantly, a meso compound will reduce the number of stereoisomers to below the hypothetical 2n amount due to symmetry.[6]
Additionally, certain configurations may not exist due to steric reasons. Cyclic compounds with chiral centers may not exhibit chirality due to the presence of a two-fold rotation axis. Planar chirality may also provide for chirality without having an actual chiral center present.
Configuration
[edit]Configuration is defined as the arrangement of atoms around a stereocenter.[6] The Cahn-Ingold-Prelog (CIP) system uses R and S designations to define the configuration of atoms about any stereocenter.[7] A designation of R denotes a clockwise direction of substituent priority around the stereocenter, while a designation of S denotes a counter-clockwise direction of substituent priority.[7]
Chirality Centers
[edit]A chirality center (chiral center) is a type of stereocenter. A chirality center is defined as an atom holding a set of four different ligands (atoms or groups of atoms) in a spatial arrangement which is non-superposable on its mirror image. Chirality centers must be sp3 hybridized, meaning that a chirality center can only have single bonds.[5] In organic chemistry, a chirality center usually refers to a carbon, phosphorus, or sulfur atom, though it is also possible for other atoms to be chirality centers, especially in areas of organometallic and inorganic chemistry.
The concept of a chirality center generalizes the concept of an asymmetric carbon atom (a carbon atom bonded to four different entities) to a broader definition of any atom with four different attachment groups in which an interchanging of any two attachment groups gives rise to an enantiomer.[8]
Stereogenic on Carbon
[edit]A carbon atom that is attached to four different substituent groups is called an asymmetric carbon atom or chiral carbon. Chiral carbons are the most common type of chirality center.[6]
Stereogenic on Other Atoms
[edit]Chirality is not limited to carbon atoms, though carbon atoms are often centers of chirality due to their ubiquity in organic chemistry. Nitrogen and phosphorus atoms can also form bonds in a tetrahedral configuration. A nitrogen in an amine may be a stereocenter if all three groups attached are different because the electron pair of the amine functions as a fourth group.[9] However, nitrogen inversion, a form of pyramidal inversion, causes racemization which means that both epimers at that nitrogen are present under normal circumstances.[9] Racemization by nitrogen inversion may be restricted (such as quaternary ammonium or phosphonium cations), or slow, which allows the existence of chirality.[9]
Metal atoms with tetrahedral or octahedral geometries may also be chiral due to having different ligands. For the octahedral case, several chiralities are possible. Having three ligands of two types, the ligands may be lined up along the meridian, giving the mer-isomer, or forming a face—the fac isomer. Having three bidentate ligands of only one type gives a propeller-type structure, with two different enantiomers denoted Λ and Δ.
Chirality and Stereocenters
[edit]As mentioned earlier, the requirement for an atom to be a chirality center is that the atom must be sp3 hybridized with four different attachments.[5] Because of this, all chirality centers are stereocenters. However, only under some conditions is the reverse true. Recall that a point can be considered a sterocenter with a minimum of three attachment points; stereocenters can be either sp3 or sp2 hybridized, as long as the interchanging any two different groups creates a new stereoisomer. This means that although all chirality centers are stereocenters, not every stereocenter is a chirality center.
Stereocenters are important identifiers for chiral or achiral molecules. As a general rule, if a molecule has no stereocenters, it is considered achiral. If it has at least one stereocenter, the molecule has the potential for chirality. However, there are some exceptions like meso compounds that make molecules with multiple stereocenters considered achiral.[6]
See also
[edit]- Chirality (chemistry) § Stereogenic centers
- Cahn–Ingold–Prelog priority rules for nomenclature
- Descriptor (chemistry)
References
[edit]- ^ a b c "5.4: Stereogenic Centers". libretexts.org. April 24, 2015.
- ^ a b Mislow, Kurt; Siegel, Jay (1984). "Stereoisomerism and local chirality". Journal of the American Chemical Society. 106 (11): 3319. doi:10.1021/ja00323a043.
- ^ a b Solomons, T. W. Graham; Fryhle, Craig (2004). Organic Chemistry (8th ed.). John Wiley & Sons.[page needed]
- ^ a b Soderberg, Timothy (July 1, 2019). "Organic Chemistry with a Biological Emphasis Volume I". Chemistry Publications: 170, 177.
- ^ a b c "5.3: Chirality and R/S Naming System". Chemistry LibreTexts. December 15, 2021. Retrieved November 12, 2022.
- ^ a b c d e f Brown, William; Iverson, Brent; Anslyn, Eric; Foote, Christopher (2018). Organic Chemistry (8th ed.). Boston, MA: Cengage Learning. pp. 117, 137–139. ISBN 978-1-305-58035-0.
- ^ a b Barta, Nancy S.; Stille, John R. (1994). "Grasping the Concepts of Stereochemistry". Journal of Chemical Education. 71 (1): 20. Bibcode:1994JChEd..71...20B. doi:10.1021/ed071p20. ISSN 0021-9584.
- ^ "chiral (chirality) center". IUPAC.org. doi:10.1351/goldbook.C01060.
- ^ a b c Smith, Janice Gorzynski (2011). "Chapter 25 Amines". In Hodge, Tami; Nemmers, Donna; Klein, Jayne (eds.). Organic chemistry (Book) (3rd ed.). New York, NY: McGraw-Hill. pp. 949–993. ISBN 978-0-07-337562-5.